Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota
Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide...
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container_title | International journal of biological macromolecules |
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creator | Chen, Yanlan Huang, Junyuan Wang, Huaixu Cui, Haohui Liang, Zizhao Huang, Darong Deng, Xinyu Du, Bing Li, Pan |
description | Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. In addition, SISP altered the intestinal flora imbalance in HSD mice by reducing the relative abundance of the genera, Akkermansia, Faecalibaculum, and unidentified_Ruminococcaceae, and reversing the decline in the levels of the genera, Lactobacillus and Bacteroides. In conclusion, SISP is a promising nutraceutical for renal fibrosis management. |
doi_str_mv | 10.1016/j.ijbiomac.2024.136039 |
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This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. In addition, SISP altered the intestinal flora imbalance in HSD mice by reducing the relative abundance of the genera, Akkermansia, Faecalibaculum, and unidentified_Ruminococcaceae, and reversing the decline in the levels of the genera, Lactobacillus and Bacteroides. In conclusion, SISP is a promising nutraceutical for renal fibrosis management.</description><identifier>ISSN: 0141-8130</identifier><identifier>ISSN: 1879-0003</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.136039</identifier><identifier>PMID: 39332559</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Bacteroides ; collagen ; creatinine ; dietary supplements ; fibronectins ; Fibrosis ; Gastrointestinal Microbiome - drug effects ; gene expression ; intestinal microorganisms ; Kidney - drug effects ; Kidney - metabolism ; Kidney - pathology ; Kidney Diseases - drug therapy ; Kidney Diseases - metabolism ; Kidney Diseases - pathology ; kidneys ; Lactobacillus ; Male ; Mice ; Polysaccharides ; Polysaccharides - pharmacology ; public health ; Renal fibrosis ; renal function ; Signal Transduction - drug effects ; Smad Proteins - metabolism ; TGF-β1 ; Transforming Growth Factor beta1 - metabolism</subject><ispartof>International journal of biological macromolecules, 2024-11, Vol.280 (Pt 4), p.136039, Article 136039</ispartof><rights>2024</rights><rights>Copyright © 2024. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c278t-c7bc9d893b9822facc41bd8a214ac2db94631ce565798534598c36aae7aa5e953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijbiomac.2024.136039$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39332559$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Yanlan</creatorcontrib><creatorcontrib>Huang, Junyuan</creatorcontrib><creatorcontrib>Wang, Huaixu</creatorcontrib><creatorcontrib>Cui, Haohui</creatorcontrib><creatorcontrib>Liang, Zizhao</creatorcontrib><creatorcontrib>Huang, Darong</creatorcontrib><creatorcontrib>Deng, Xinyu</creatorcontrib><creatorcontrib>Du, Bing</creatorcontrib><creatorcontrib>Li, Pan</creatorcontrib><title>Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. In addition, SISP altered the intestinal flora imbalance in HSD mice by reducing the relative abundance of the genera, Akkermansia, Faecalibaculum, and unidentified_Ruminococcaceae, and reversing the decline in the levels of the genera, Lactobacillus and Bacteroides. In conclusion, SISP is a promising nutraceutical for renal fibrosis management.</description><subject>Animals</subject><subject>Bacteroides</subject><subject>collagen</subject><subject>creatinine</subject><subject>dietary supplements</subject><subject>fibronectins</subject><subject>Fibrosis</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>gene expression</subject><subject>intestinal microorganisms</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Kidney Diseases - drug therapy</subject><subject>Kidney Diseases - metabolism</subject><subject>Kidney Diseases - pathology</subject><subject>kidneys</subject><subject>Lactobacillus</subject><subject>Male</subject><subject>Mice</subject><subject>Polysaccharides</subject><subject>Polysaccharides - pharmacology</subject><subject>public health</subject><subject>Renal fibrosis</subject><subject>renal function</subject><subject>Signal Transduction - drug effects</subject><subject>Smad Proteins - metabolism</subject><subject>TGF-β1</subject><subject>Transforming Growth Factor beta1 - metabolism</subject><issn>0141-8130</issn><issn>1879-0003</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1uFDEQhS0EIkPgCpGXbHpit3_a3oEiEiJFAilhbVXb1bRH_TPY3aC5AAfiIJwJjyZhCyvLru9V1fMj5IKzLWdcX-62cdfGeQS_rVktt1xoJuwzsuGmsRVjTDwnG8YlrwwX7Iy8ynlXXrXi5iU5E1aIWim7IT8_z8Mhg_c9pBgw0y7NI72Hcqe3k-8jzT0OA00YVl_KCScYaBfbNOeYaZzoGD3S9kDHOawDLHH6Spce6cPNdfX7F7-8HyHQPSz9DzhQmEKRLJgLVtoUaZqLiwVekxcdDBnfPJ7n5Mv1h4erj9Xdp5vbq_d3la8bs1S-ab0NxorWmrruytqSt8FAzSX4OrRWasE9Kq0aa5SQyhovNAA2AAqtEufk7anvPs3f1rKHG2P2xSBMOK_ZCa4kb7jW8j9QzhrBpDmi-oQWOzkn7Nw-xRHSwXHmjnG5nXuKyx3jcqe4ivDiccbajhj-yp7yKcC7E4DlU75HTC77iJPHEBP6xYU5_mvGH8L8q2Q</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Chen, Yanlan</creator><creator>Huang, Junyuan</creator><creator>Wang, Huaixu</creator><creator>Cui, Haohui</creator><creator>Liang, Zizhao</creator><creator>Huang, Darong</creator><creator>Deng, Xinyu</creator><creator>Du, Bing</creator><creator>Li, Pan</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202411</creationdate><title>Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota</title><author>Chen, Yanlan ; Huang, Junyuan ; Wang, Huaixu ; Cui, Haohui ; Liang, Zizhao ; Huang, Darong ; Deng, Xinyu ; Du, Bing ; Li, Pan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c278t-c7bc9d893b9822facc41bd8a214ac2db94631ce565798534598c36aae7aa5e953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Bacteroides</topic><topic>collagen</topic><topic>creatinine</topic><topic>dietary supplements</topic><topic>fibronectins</topic><topic>Fibrosis</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>gene expression</topic><topic>intestinal microorganisms</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Kidney Diseases - drug therapy</topic><topic>Kidney Diseases - metabolism</topic><topic>Kidney Diseases - pathology</topic><topic>kidneys</topic><topic>Lactobacillus</topic><topic>Male</topic><topic>Mice</topic><topic>Polysaccharides</topic><topic>Polysaccharides - pharmacology</topic><topic>public health</topic><topic>Renal fibrosis</topic><topic>renal function</topic><topic>Signal Transduction - drug effects</topic><topic>Smad Proteins - metabolism</topic><topic>TGF-β1</topic><topic>Transforming Growth Factor beta1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Yanlan</creatorcontrib><creatorcontrib>Huang, Junyuan</creatorcontrib><creatorcontrib>Wang, Huaixu</creatorcontrib><creatorcontrib>Cui, Haohui</creatorcontrib><creatorcontrib>Liang, Zizhao</creatorcontrib><creatorcontrib>Huang, Darong</creatorcontrib><creatorcontrib>Deng, Xinyu</creatorcontrib><creatorcontrib>Du, Bing</creatorcontrib><creatorcontrib>Li, Pan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Yanlan</au><au>Huang, Junyuan</au><au>Wang, Huaixu</au><au>Cui, Haohui</au><au>Liang, Zizhao</au><au>Huang, Darong</au><au>Deng, Xinyu</au><au>Du, Bing</au><au>Li, Pan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-11</date><risdate>2024</risdate><volume>280</volume><issue>Pt 4</issue><spage>136039</spage><pages>136039-</pages><artnum>136039</artnum><issn>0141-8130</issn><issn>1879-0003</issn><eissn>1879-0003</eissn><abstract>Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. In addition, SISP altered the intestinal flora imbalance in HSD mice by reducing the relative abundance of the genera, Akkermansia, Faecalibaculum, and unidentified_Ruminococcaceae, and reversing the decline in the levels of the genera, Lactobacillus and Bacteroides. In conclusion, SISP is a promising nutraceutical for renal fibrosis management.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39332559</pmid><doi>10.1016/j.ijbiomac.2024.136039</doi></addata></record> |
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subjects | Animals Bacteroides collagen creatinine dietary supplements fibronectins Fibrosis Gastrointestinal Microbiome - drug effects gene expression intestinal microorganisms Kidney - drug effects Kidney - metabolism Kidney - pathology Kidney Diseases - drug therapy Kidney Diseases - metabolism Kidney Diseases - pathology kidneys Lactobacillus Male Mice Polysaccharides Polysaccharides - pharmacology public health Renal fibrosis renal function Signal Transduction - drug effects Smad Proteins - metabolism TGF-β1 Transforming Growth Factor beta1 - metabolism |
title | Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota |
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